tadalafil
Generic: tadalafil
Labeler: avkareDrug Facts
Product Profile
Brand Name
tadalafil
Generic Name
tadalafil
Labeler
avkare
Dosage Form
TABLET
Routes
Active Ingredients
tadalafil 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
73190-032
Product ID
73190-032_3c1c1b65-f5b9-62b0-e063-6294a90a1021
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210608
Listing Expiration
2026-12-31
Marketing Start
2025-08-11
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73190032
Hyphenated Format
73190-032
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
tadalafil (source: ndc)
Generic Name
tadalafil (source: ndc)
Application Number
ANDA210608 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 60 TABLET in 1 BOTTLE (73190-032-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c1c1b65-f5b9-62b0-e063-6294a90a1021", "openfda": {"nui": ["N0000175599", "N0000020026"], "upc": ["0373190032602"], "unii": ["742SXX0ICT"], "rxcui": ["2123194"], "spl_set_id": ["3c1c2136-099f-6232-e063-6294a90a6975"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (73190-032-60)", "package_ndc": "73190-032-60", "marketing_start_date": "20250811"}], "brand_name": "TADALAFIL", "product_id": "73190-032_3c1c1b65-f5b9-62b0-e063-6294a90a1021", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "73190-032", "generic_name": "tadalafil", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TADALAFIL", "active_ingredients": [{"name": "TADALAFIL", "strength": "20 mg/1"}], "application_number": "ANDA210608", "marketing_category": "ANDA", "marketing_start_date": "20250811", "listing_expiration_date": "20261231"}